Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397514262
rs397514262
ERBB4
1 1.000 2 211424241 missense variant C/T snv 1.6E-05 1.4E-05 0.800 1.000 1 2013 2013
dbSNP: rs397514263
rs397514263
ERBB4
1 1.000 2 211383719 missense variant G/A snv 4.0E-05 7.0E-06 0.800 1.000 1 2013 2013